Exactech, Inc. recalls Optetrak Constrained Condylar Offset Screw, Size KK, Ref 208
See all recalls from Exactech, Inc. →Recalled Product
Optetrak Constrained Condylar Offset Screw, Size KK, Ref 208-04-78, Sterile, RX.
Hazard / Issue
There is a design incompatibility between certain sizes of the offset spine stiffener screw and the constrained condylar tibial insert when used in conjunction with an offset tibial tray.
Issued by
FDA
Affected States: AL, FL, IN, ME, MN, NJ, NY, OH, OK, VA
Lot/Code Info: All lot numbers
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Optetrak Constrained Condylar Offset →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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